Pure Global

"Kendalo" components for in vitro limb prosthetics (unsterilized) - Taiwan Registration 895c099b5dc42efc7e773a32aac419a1

Access comprehensive regulatory information for "Kendalo" components for in vitro limb prosthetics (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 895c099b5dc42efc7e773a32aac419a1 and manufactured by KEN DALL ENTERPRISE CO., LTD.. The authorized representative in Taiwan is KEN DALL ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free Database
Powered by Pure Global AI
89,000+ Devices
895c099b5dc42efc7e773a32aac419a1
Registration Details
Taiwan FDA Registration: 895c099b5dc42efc7e773a32aac419a1
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Kendalo" components for in vitro limb prosthetics (unsterilized)
TW: โ€œ่‚ฏ้”่ทฏโ€ ้ซ”ๅค–่‚ข้ซ”็พฉ่‚ข็”จ็ต„ไปถ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

895c099b5dc42efc7e773a32aac419a1

Company Information

Taiwan, Province of China

Product Details

Limited to the classification and grading management method of medical equipment, in vitro limb prosthetic components (O.3420) the first level recognition range.

o Physical Medical Sciences

O.3420 ้ซ”ๅค–่‚ข้ซ”็พฉ่‚ข็”จ็ต„ไปถ

Domestic

Dates and Status

Oct 01, 2021

Oct 31, 2025